Defining the heterochromatin localization and repression domains of SALL1

2006 | journal article. A publication with affiliation to the University of Göttingen.

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​Defining the heterochromatin localization and repression domains of SALL1​
Netzer, C.; Bohlander, S. K.; Hinzke, M.; Chen, Y. & Kohlhase, J.​ (2006) 
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease1762(3) pp. 386​-391​.​ DOI: https://doi.org/10.1016/j.bbadis.2005.12.005 

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Authors
Netzer, C.; Bohlander, S. K.; Hinzke, M.; Chen, Y.; Kohlhase, Juergen
Abstract
SALL1 has been identified as one of four human homologues of the Drosophila region-specific homeotic gene spalt (sal), encoding zinc finger proteins of characteristic structure. Mutations of SALL1 on chromosome 16q12.1 cause Townes-Brocks syndrome (TBS, OMIM 107480). We have shown previously that SALL1 acts as a strong transcriptional repressor in mammalian cells when fused to a heterologous DNA-binding domain. Here, we report that SALL1 contains two repression domains, one located at the extreme N-terminus of the protein and the other in the central region. SALL1 fragments with the central repression domain exhibited a punctate nuclear distribution pattern at pericentromeric heterochromatin foci in murine NIH-3T3 cells, suggesting an association between repression and heterochromatin localization. The implications of these findings for the pathogenesis of Townes-Brocks syndrome are discussed. (c) 2005 Elsevier B.V. All rights reserved.
Issue Date
2006
Status
published
Publisher
Elsevier Science Bv
Journal
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 
ISSN
0925-4439

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